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    Gangwal Healthcare is powered by innovation, driving health, wellness & healing.

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    SPI Pharma has been solving formulation challenges using superior functional materials.

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    Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.

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    HYDROMORPHONE HCL

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    01 5Actavis Inc

    02 8Ajanta Pharma Limited

    03 4Apotex Inc

    04 2Ascent Pharmaceuticals

    05 3Aurolife Pharma LLC

    06 1Barr Laboratories

    07 4Chartwell Pharmaceuticals llc

    08 4Farbe Firma

    09 2Fresenius Kabi Austria

    10 7Fresenius Kabi USA

    11 3GL Pharma

    12 4HAMELN PHARMA PTY. LTD.

    13 3Hana Pharm

    14 9Hikma Pharmaceuticals

    15 7Hospira, Inc.

    16 1JAMP PHARMA

    17 5Janssen-Cilag

    18 5Johnson & Johnson Innovative Medicine

    19 4Juno Pharmaceuticals Pty Ltd

    20 2Lannett Company, Inc.

    21 3Link Healthcare

    22 15Mallinckrodt Pharmaceuticals

    23 10Medsurge Healthcare

    24 49Mundipharma

    25 3Nesher Pharmaceuticals USA LLC

    26 1Nostrum Laboratories

    27 4Osmotica Pharmaceuticals

    28 4Padagis

    29 1Pfizer Inc

    30 11Pharmascience Inc.

    31 12Purdue Pharma

    32 4Purdue Pharmaceuticals L.P

    33 4RHODES PHARMACEUTICALS LP

    34 2Rising Pharmaceuticals Inc

    35 4STERIMAX INC

    36 5Sandoz B2B

    37 2Sterinova Inc.

    38 1Streuli Pharma

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    01

    Actavis Inc

    Ireland
    The Pharmacy Technology
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    Actavis Inc

    Ireland
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : HYDROMORPHONE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 1995-08-23

    Application Number : 74317

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Fresenius Kabi USA

    U.S.A
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    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID-HP

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 1984-01-11

    Application Number : 19034

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Fresenius Kabi USA

    U.S.A
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    Not Confirmed
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    U.S.A
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    Regulatory Info : DISCN

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID-HP

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 250MG/VIAL

    Packaging :

    Approval Date : 1994-08-04

    Application Number : 19034

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : RX

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1MG/ML

    Packaging :

    Approval Date : 2009-04-30

    Application Number : 19034

    Regulatory Info : RX

    Registration Country : USA

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    05

    Fresenius Kabi USA

    U.S.A
    The Pharmacy Technology
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 2MG/ML

    Packaging :

    Approval Date : 2009-04-30

    Application Number : 19034

    Regulatory Info : RX

    Registration Country : USA

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    06

    Fresenius Kabi USA

    U.S.A
    The Pharmacy Technology
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : RX

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 4MG/ML

    Packaging :

    Approval Date : 2009-04-30

    Application Number : 19034

    Regulatory Info : RX

    Registration Country : USA

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    07

    Fresenius Kabi USA

    U.S.A
    The Pharmacy Technology
    Not Confirmed
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    Fresenius Kabi USA

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    Regulatory Info : RX

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.2MG/ML

    Packaging :

    Approval Date : 2020-01-16

    Application Number : 19034

    Regulatory Info : RX

    Registration Country : USA

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    08

    Fresenius Kabi USA

    U.S.A
    The Pharmacy Technology
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    The Pharmacy Technology
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    Regulatory Info : RX

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.5MG/0.5ML

    Packaging :

    Approval Date : 2017-02-10

    Application Number : 19034

    Regulatory Info : RX

    Registration Country : USA

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    09

    Mallinckrodt Pharmaceuticals

    Ireland
    The Pharmacy Technology
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    Mallinckrodt Pharmaceuticals

    Ireland
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    Regulatory Info : DISCN

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : EXALGO

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2010-03-01

    Application Number : 21217

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Mallinckrodt Pharmaceuticals

    Ireland
    The Pharmacy Technology
    Not Confirmed
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    Mallinckrodt Pharmaceuticals

    Ireland
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    The Pharmacy Technology
    Not Confirmed
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    Regulatory Info : DISCN

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : EXALGO

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2010-03-01

    Application Number : 21217

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Mallinckrodt Pharmaceuticals

    Ireland
    The Pharmacy Technology
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : EXALGO

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 16MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2010-03-01

    Application Number : 21217

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Mallinckrodt Pharmaceuticals

    Ireland
    The Pharmacy Technology
    Not Confirmed
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    Mallinckrodt Pharmaceuticals

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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : EXALGO

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 32MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2012-08-24

    Application Number : 21217

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Purdue Pharmaceuticals L.P

    U.S.A
    The Pharmacy Technology
    Not Confirmed
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    Purdue Pharmaceuticals L.P

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : PALLADONE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 12MG

    Packaging :

    Approval Date : 2004-09-24

    Application Number : 21044

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Purdue Pharmaceuticals L.P

    U.S.A
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    Regulatory Info : DISCN

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : PALLADONE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 16MG

    Packaging :

    Approval Date : 2004-09-24

    Application Number : 21044

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Purdue Pharmaceuticals L.P

    U.S.A
    The Pharmacy Technology
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    Regulatory Info : DISCN

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : PALLADONE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 24MG

    Packaging :

    Approval Date : 2004-09-24

    Application Number : 21044

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Purdue Pharmaceuticals L.P

    U.S.A
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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : PALLADONE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 32MG

    Packaging :

    Approval Date : 2004-09-24

    Application Number : 21044

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    RHODES PHARMACEUTICALS LP

    U.S.A
    The Pharmacy Technology
    Not Confirmed
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    RHODES PHARMACEUTICALS LP

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 5MG/5ML

    Packaging :

    Approval Date : 1992-12-07

    Application Number : 19891

    Regulatory Info : RX

    Registration Country : USA

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    18

    RHODES PHARMACEUTICALS LP

    U.S.A
    The Pharmacy Technology
    Not Confirmed
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    RHODES PHARMACEUTICALS LP

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    Regulatory Info : RX

    Registration Country : USA

    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 8MG

    Packaging :

    Approval Date : 1992-12-07

    Application Number : 19892

    Regulatory Info : RX

    Registration Country : USA

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    19

    RHODES PHARMACEUTICALS LP

    U.S.A
    The Pharmacy Technology
    Not Confirmed
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    RHODES PHARMACEUTICALS LP

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 4MG

    Packaging :

    Approval Date : 2007-11-09

    Application Number : 19892

    Regulatory Info : RX

    Registration Country : USA

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    20

    RHODES PHARMACEUTICALS LP

    U.S.A
    The Pharmacy Technology
    Not Confirmed
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    RHODES PHARMACEUTICALS LP

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Packaging :

    Approval Date : 2007-11-09

    Application Number : 19892

    Regulatory Info : RX

    Registration Country : USA

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